A study of voice and non-voice processing in Prader-Willi syndrome

BACKGROUND: Prader-Willi syndrome (PWS) is a rare and complex neurodevelopmental disorder of genetic origin. It manifests itself in endocrine and cognitive problems, including highly pronounced hyperphagia and severe obesity. In many cases, impaired acquisition of social and communication skills lea...

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Detalles Bibliográficos
Autores principales: Strenilkov, Kuzma, Debladis, Jimmy, Salles, Juliette, Valette, Marion, Mantoulan, Carine, Thuilleaux, Denise, Laurier, Virginie, Molinas, Catherine, Barone, Pascal, Tauber, Maïthé
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972021/
https://www.ncbi.nlm.nih.gov/pubmed/31959191
http://dx.doi.org/10.1186/s13023-020-1298-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972021/
https://www.ncbi.nlm.nih.gov/pubmed/31959191
http://dx.doi.org/10.1186/s13023-020-1298-8

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